Use the force, fluke: Ligand-independent gating of Schistosoma mansoni ion channel TRPMPZQ

Int J Parasitol. 2023 Jul;53(8):427-434. doi: 10.1016/j.ijpara.2022.11.004. Epub 2023 Jan 4.


The parasitic flatworm ion channel, TRPMPZQ, is a non-selective cation channel that mediates Ca2+ entry and membrane depolarization when activated by the anthelmintic drug, praziquantel (PZQ). TRPMPZQ is conserved in all platyhelminth genomes scrutinized to date, with the sensitivity of TRPMPZQ in any particular flatworm correlating with the overall sensitivity of the worm to PZQ. Conservation of this channel suggests it plays a role in flatworm physiology, but the nature of the endogenous cues that activate this channel are currently unknown. Here, we demonstrate that TRPMPZQ is activated in a ligand-independent manner by membrane stretch, with the electrophysiological signature of channel opening events being identical whether evoked by negative pressure, or by PZQ. TRPMPZQ is therefore a multimodal ion channel gated by both physical and chemical cues. The mechanosensitivity of TRPMPZQ is one route for endogenous activation of this ion channel that holds relevance for schistosome physiology given the persistent pressures and mechanical cues experienced throughout the parasite life cycle.

Keywords: Anthelmintic; Electrophysiology; Ion channel; Mechanosensitivity; Parasite.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenosine Diphosphate Ribose / metabolism
  • Animals
  • Helminth Proteins* / metabolism
  • Humans
  • Pressure
  • Schistosoma mansoni*
  • TRPM Cation Channels* / metabolism


  • TRPM Cation Channels
  • Helminth Proteins
  • Adenosine Diphosphate Ribose